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首页> 外文期刊>Development >Zeste maintains repression of Ubx transgenes: support for a new model of Polycomb repression.
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Zeste maintains repression of Ubx transgenes: support for a new model of Polycomb repression.

机译:Zeste维持对Ubx转基因的抑制:支持一种新型的Polycomb抑制模型。

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摘要

During late embryogenesis, the expression domains of homeotic genes are maintained by two groups of ubiquitously expressed regulators: the Polycomb repressors and the Trithorax activators. It is not known how the activities of the two maintenance systems are initially targeted to the correct genes. Zeste and GAGA are sequence-specific DNA-binding proteins previously shown to be Trithorax group activators of the homeotic gene Ultrabithorax (Ubx). We demonstrate that Zeste and GAGA DNA-binding sites at the proximal promoter are also required to maintain, but not to initiate, repression of UBX: Furthermore, the repression mediated by Zeste DNA-binding site is abolished in zeste null embryos. These data imply that Zeste and probably GAGA mediate Polycomb repression. We present a model in which the dual transcriptional activities of Zeste and GAGA are an essential component of the mechanism that chooses which maintenance system is to be targeted to a given promoter.
机译:在晚期胚胎发生过程中,同源基因的表达域由两组无处不在的调节子维持:Polycomb阻遏物和Trithorax激活物。尚不知道两个维护系统的活动最初如何针对正确的基因。 Zeste和GAGA是序列特异性的DNA结合蛋白,以前被证明是同源基因Ultrabithorax(Ubx)的Trithorax基团激活剂。我们证明,近端启动子的Zeste和GAGA DNA结合位点也需要维持而不是启动UBX的抑制:此外,在zeste null胚胎中废除了Zeste DNA结合位点介导的抑制。这些数据表明Zeste和GAGA可能会介导Polycomb压制。我们提出了一个模型,其中Zeste和GAGA的双重转录活性是选择哪个维护系统针对给定启动子的机制的基本组成部分。

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